Long non-coding RNAs drive metastatic progression in melanoma (Review)

被引:11
作者
Akhbari, Pouria [1 ]
Whitehouse, Adrian [2 ,3 ]
Boyne, James R. [1 ]
机构
[1] Univ Bradford, Ctr Skin Sci, Bradford BD7 1DP, W Yorkshire, England
[2] Univ Leeds, Fac Biol Sci, Sch Mol & Cellular Biol, Leeds, W Yorkshire, England
[3] Univ Leeds, Astbury Ctr Struct Mol Biol, Leeds, W Yorkshire, England
基金
英国生物技术与生命科学研究理事会;
关键词
melanoma; long non-coding RNA; metastasis; EPITHELIAL-MESENCHYMAL TRANSITION; POOR-PROGNOSIS; PROMOTES METASTASIS; CELL-PROLIFERATION; HUMAN GENOME; PSF PROTEIN; VL30; RNA; HOTAIR; GENE; TRANSCRIPTION;
D O I
10.3892/ijo.2014.2691
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastatic melanoma is the leading cause of skin-cancer related deaths and while in recent years some progress has been made with targeted therapies, there remains an urgent unmet need for novel therapeutic treatments and reliable diagnostic, prognostic and predictive biomarkers. The emergence of next generation sequencing (NGS) has seen a growing appreciation for the role played by non-coding genomic transcripts in regulating gene expression and by extension impacting on disease progression. The long non-coding RNAs (IncRNAs) represent the most enigmatic of these new regulatory molecules. Our understanding of how IncRNAs regulate biological functions and their importance to disease aetiology, while still limited, is rapidly improving, in particular with regards to their role in cancer. Herein we review the identification of several IncRNAs shown to impact on melanoma disease progression and discuss how these molecules are operating at the molecular level.
引用
收藏
页码:2181 / 2186
页数:6
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